Yu Abe

1.2k total citations · 1 hit paper
24 papers, 825 citations indexed

About

Yu Abe is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Yu Abe has authored 24 papers receiving a total of 825 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Neurology. Recurrent topics in Yu Abe's work include RNA modifications and cancer (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Hedgehog Signaling Pathway Studies (3 papers). Yu Abe is often cited by papers focused on RNA modifications and cancer (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Hedgehog Signaling Pathway Studies (3 papers). Yu Abe collaborates with scholars based in Japan, United States and Australia. Yu Abe's co-authors include Yoko Aoki, Yoichi Matsubara, Shigeo Kure, Tetsuya Niihori, Atsuo Kikuchi, Shigeru Tsuchiya, Naoto Ishii, Yoichi Suzuki, Teiji Tominaga and Yuji Owada and has published in prestigious journals such as Biological Psychiatry, Journal of Hepatology and Developmental Medicine & Child Neurology.

In The Last Decade

Yu Abe

23 papers receiving 814 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A genome-wide association study identifies RNF213 as the first Moyamoya disease gene

2010 514 citations Fumiaki Kamada, Yoko Aoki et al. Journal of Human Genetics profile →

Peers

Yu Abe

RHEUM

NEURO

PMH

GENET

Junko Kanno Japan

Shoko Komatsuzaki Germany

Guilhem Solé France

Kimihiko Kaneko Japan

Jukka Loukkola Finland

Seung‐Ki Kim South Korea

Mark Woodhall United Kingdom

J. He China

K D MacDermot United Kingdom

Philippe Kerschen France

Junko Kanno Japan

Yu Abe

487 ×1.0

RHEUM

329 ×1.0

NEURO

240 ×0.9

PMH

264 ×1.0

188 ×1.3

GENET

Citations per year, relative to Yu Abe Yu Abe (= 1×) peers Junko Kanno

Countries citing papers authored by Yu Abe

Since Specialization

Citations

This map shows the geographic impact of Yu Abe's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Yu Abe with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Yu Abe more than expected).

Fields of papers citing papers by Yu Abe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yu Abe. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Yu Abe. The network helps show where Yu Abe may publish in the future.

Co-authorship network of co-authors of Yu Abe

This figure shows the co-authorship network connecting the top 25 collaborators of Yu Abe. A scholar is included among the top collaborators of Yu Abe based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Yu Abe. Yu Abe is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Kobayashi, Tomoko, Yoshitsugu Oikawa, Yu Abe, et al.. (2023). A Case Series of Patients With MYBPC1 Gene Variants Featuring Undulating Tongue Movements as Myogenic Tremor. Pediatric Neurology. 146. 16–20. 4 indexed citations

Abe, Yu, et al.. (2022). Successful treatment with dimethyl fumarate in a child with relapsing-remitting multiple sclerosis. Brain and Development. 44(5). 353–356. 2 indexed citations

Shirota, Matsuyuki, Atsuo Kikuchi, Yu Abe, et al.. (2022). A novel variant in the transmembrane 4 domain of ANO3 identified in a two-year-old girl with developmental delay and tremor. Journal of Human Genetics. 68(1). 51–54. 3 indexed citations

Abe, Yu, Wakaba Endo, Hiroshi Hasegawa, et al.. (2021). The effect of dietary protein restriction in a case of molybdenum cofactor deficiency with MOCS1 mutation. Molecular Genetics and Metabolism Reports. 26. 100716–100716. 10 indexed citations

Deng, Xi, et al.. (2019). Uncertainty quantification of shock–bubble interaction simulations. Shock Waves. 29(8). 1191–1204. 2 indexed citations

Nakamura, Haruhiko, Mitsugu Uematsu, Yu Abe, et al.. (2018). Rett-like features and cortical visual impairment in a Japanese patient with HECW2 mutation. Brain and Development. 40(5). 410–414. 7 indexed citations

Roessler, Erich, Ping Hu, Sung‐Kook Hong, et al.. (2018). Common genetic causes of holoprosencephaly are limited to a small set of evolutionarily conserved driver genes of midline development coordinated by TGF-β, hedgehog, and FGF signaling. Human Mutation. 39(10). 1416–1427. 19 indexed citations

Abe, Yu, Paul Kruszka, Ariel F. Martinez, et al.. (2018). Clinical and Demographic Evaluation of a Holoprosencephaly Cohort From the Kyoto Collection of Human Embryos. The Anatomical Record. 301(6). 973–986. 10 indexed citations

Martinez, Ariel F., Yu Abe, Paul Kruszka, et al.. (2017). Human germline hedgehog pathway mutations predispose to fatty liver. Journal of Hepatology. 67(4). 809–817. 25 indexed citations

10.

Martinez, Ariel F., Yu Abe, Sung‐Kook Hong, et al.. (2016). An Ultraconserved Brain-Specific Enhancer Within ADGRL3 (LPHN3) Underpins Attention-Deficit/Hyperactivity Disorder Susceptibility. Biological Psychiatry. 80(12). 943–954. 45 indexed citations

11.

Abe, Yu, Atsuo Kikuchi, Satoru Kobayashi, et al.. (2014). Xq26.1‐26.2 gain identified on array comparative genomic hybridization in bilateral periventricular nodular heterotopia with overlying polymicrogyria. Developmental Medicine & Child Neurology. 56(12). 1221–1224. 12 indexed citations

12.

Wakusawa, Keisuke, Satoru Kobayashi, Yu Abe, et al.. (2013). A girl with Cardio-facio-cutaneous syndrome complicated with status epilepticus and acute encephalopathy. Brain and Development. 36(1). 61–63. 8 indexed citations

13.

Haginoya, Kazuhiro, Mitsugu Uematsu, Mitsutoshi Munakata, et al.. (2013). The usefulness of subtraction ictal SPECT and ictal near-infrared spectroscopic topography in patients with West syndrome. Brain and Development. 35(10). 887–893. 7 indexed citations

14.

Abe, Yu, Yoko Aoki, Shinichi Kuriyama, et al.. (2012). Prevalence and clinical features of Costello syndrome and cardio‐facio‐cutaneous syndrome in Japan: Findings from a nationwide epidemiological survey. American Journal of Medical Genetics Part A. 158A(5). 1083–1094. 63 indexed citations

15.

Adachi, Masao, Yu Abe, Yoko Aoki, & Yoichi Matsubara. (2011). Epilepsy in RAS/MAPK syndrome: Two cases of cardio-facio-cutaneous syndrome with epileptic encephalopathy and a literature review. Seizure. 21(1). 55–60. 26 indexed citations

16.

Izumi, Rumiko, Naoki Suzuki, Takafumi Hasegawa, et al.. (2011). A Case of Late Onset Riboflavin-responsive Multiple Acyl-CoA Dehydrogenase Deficiency Manifesting as Recurrent Rhabdomyolysis and Acute Renal Failure. Internal Medicine. 50(21). 2663–2668. 28 indexed citations

17.

Kamada, Fumiaki, Yoko Aoki, Ayumi Narisawa, et al.. (2010). A genome-wide association study identifies RNF213 as the first Moyamoya disease gene. Journal of Human Genetics. 56(1). 34–40. 514 indexed citations breakdown →

18.

Uematsu, Mitsugu, Kazuhiro Haginoya, Noriko Togashi, et al.. (2010). Unique discrepancy between cerebral blood flow and glucose metabolism in hemimegalencephaly. Epilepsy Research. 92(2-3). 201–208. 10 indexed citations

19.

Uematsu, Mitsugu, Yu Abe, Keisuke Wakusawa, et al.. (2010). [High dose of enzyme replacement therapy was successful for the pulmonary involvement in a case of type 2 Gaucher disease].. PubMed. 42(1). 45–9.

20.

Funato, Tadao, Noriyuki Satoh, Yu Abe, et al.. (2001). Quantitative PCR determination of human cytomegalovirus in blood cells. Journal of Clinical Laboratory Analysis. 15(3). 122–126. 7 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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